Variant #0000888477 (NC_000008.10:g.94772179G>T, NC_000008.10(NM_153704.5):c.406+1375G>T (TMEM67))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.94772179G>T
DNA change (hg38) -
Published as TMEM67(NM_001142301.1):c.121G>T (p.(Ala41Ser))
ISCN -
DB-ID TMEM67_000219
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00113 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM67 NM_153704.5 -?/. - c.406+1375G>T r.(=) p.(=)


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